MP Research
Testing & Documentation Standards
- Batch records should include product name, SKU, batch/lot number, test method, laboratory, test date, and report revision status.
- COA and supporting analysis documents should be retained as originally issued and linked to the corresponding batch or lot.
- Superseded, withdrawn, or corrected reports should remain traceable and clearly marked.
- Product claims should be limited to documented analytical, identity, purity, composition, storage, and research-use information.
- Any customer-facing quality claim should be supported by retained documentation before publication.
This page is operational guidance and is not legal, regulatory, medical, tax, banking, or shipping advice. Product-by-product review by qualified counsel and compliance professionals is recommended before sale.